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1262210-29-6

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  • 1262210-29-6 Structure

  • Basic information

    1. Product Name: 2-(6-methoxycyclohex-1-en-1-yl)naphthalene
    2. Synonyms: 2-(6-methoxycyclohex-1-en-1-yl)naphthalene
    3. CAS NO:1262210-29-6
    4. Molecular Formula:
    5. Molecular Weight: 238.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1262210-29-6.mol
    9. Article Data: 1

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(6-methoxycyclohex-1-en-1-yl)naphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(6-methoxycyclohex-1-en-1-yl)naphthalene(1262210-29-6)
    11. EPA Substance Registry System: 2-(6-methoxycyclohex-1-en-1-yl)naphthalene(1262210-29-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1262210-29-6(Hazardous Substances Data)

1262210-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262210-29-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,2,1 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1262210-29:
(9*1)+(8*2)+(7*6)+(6*2)+(5*2)+(4*1)+(3*0)+(2*2)+(1*9)=106
106 % 10 = 6
So 1262210-29-6 is a valid CAS Registry Number.

1262210-29-6Downstream Products

1262210-29-6Relevant articles and documents

Synthesis of polysubstituted olefins by Pd-catalyzed cross-coupling reaction of tosylhydrazones and aryl nonaflates

Barluenga, Jose,Florentino, Lucia,Aznar, Fernando,Valdes, Carlos

supporting information; experimental part, p. 510 - 513 (2011/03/22)

Aryl nonaflates are employed as electrophiles in the Pd-catalyzed cross-coupling with tosylhydrazones affording di-, tri-, and tetrasubstituted olefins. Fine tunning of the reaction conditions are required to accomplish the coupling successfully, includin

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